A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2749864



Internal ID10330834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:72275538..72276394hg38UCSC Ensembl
Outerchr15:72567879..72568735hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38857
hg19857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6851889, essv6867703, essv6820213, essv6673858, essv6862912, essv6966480, essv6755894, essv6665342, essv6959996, essv6857883, essv6713676, essv6761282, essv6735459, essv6766023, essv6763655, essv6936606, essv6752869
SamplesSSM027, SSM087, SSM088, SSM057, SSM058, SSM021, SSM061, SSM029, SSM062, SSM026, SSM089, SSM031, SSM086, SSM006, SSM078, SSM049, SSM063
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2749864
Frequency
Sample Size96
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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